- Ведение проектов по разработке и выводу на рынок новых продуктов от появления идеи до полной ее проработки и реализации; - Проведение профильных обзоров российского и международного рынков аналогичных продуктов (самостоятельно и с помощью отдела маркетинга); - Взаимодействие с внутренними подразделениями компании (лаборатория, производство, контроль качества, маркетинг и другие) и с внешними партнерами (поставщики сырья и упаковки, дизайнеры и полиграфисты) по всем вопросам, касающимся создания и вывода на рынок нового продукта; - Взаимодействие с зарубежными производственными и сырьевыми компаниями по поводу возможного сотрудничества, поставки образцов их продукции, ведение; - Управление проектом по выводу новой продукции: написание и защита проекта, определение и контроль сроков проведения активностей по проекту, оценка рисков, управление проектной командой.

Product program support

Rotations in Medical Dpt

Research work "Interaction between dormant forms of E. coli K12 with cells of innate immune system" Methods: RT-PCR, ELISA, isolation of DNA and RNA, reverse transcription, electrophoresis, analysis of English literature. The result: thesis, graduate work

· Complaints handling. · Perform activities within QMS (change control, CAPA, deviations, recall). · Interaction with suppliers of standards and reagents for certification / declaration and selective control; · Define, review and participate in risks assessments, investigations or corrective and preventive actions (CAPA) of product complaints, failures, recalls, withdrawals and quality related problems · Interaction with laboratories for the needs of standards and reagents; · Interaction with logistics and registration units to determine the need for standards and reagents, taking into account delivery plans; · Full cycle of procurement of standards and reagents, tracking of orders; · Inventory of purchased standards, reagents and equipment; · Coordination with the logistics and customs department for import of standards and reagents; · Translation of documents, preparation of a package of documents necessary for obtaining an import permit; · Accounting and maintenance of temperature deviations.

· Quality control of drugs in accordance with the manufacturer's pharmacopoeial monograph; · Validation of methods of analysis; · Stability study under room temperature and accelerated stability study · Study implementation and processing of the results; · Participation in bottling of experimental prototypes of sterile drugs; · Familiarization with technological documentation

Research work "The functional significance of T-cadherin gene polymorphism (CDH13) and its role in the development and manifestation of coronary heart disease " Methods: RT-PCR, ELISA, isolation of DNA and RNA, reverse transcription, western-blot, sequence analysis, spectrophotometry, analysis of English literature. The result: course work Publication “T-cadherin gene polymorphism (CDH13) associates with manifestation of coronary heart disease” (biomedical journal of Pirogov RNRMU “Bulletin of RSMU”)